ZMP
dnajc11
Ensembl ID:
ZFIN ID:
Description:
DnaJ (Hsp40) homolog, subfamily C, member 11 [Source:RefSeq peptide;Acc:NP_997796]
Human Orthologue:
DNAJC11
Human Description:
DnaJ (Hsp40) homolog, subfamily C, member 11 [Source:HGNC Symbol;Acc:25570]
Mouse Orthologue:
Dnajc11
Mouse Description:
DnaJ (Hsp40) homolog, subfamily C, member 11 Gene [Source:MGI Symbol;Acc:MGI:2443386]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16194 | Nonsense | Available for shipment | Available now |
sa9129 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24367 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16194
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016096 | Nonsense | 273 | 563 | 8 | 16 |
Genomic Location (Zv9):
Chromosome 23 (position 30954663)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 30789553 |
GRCz11 | 23 | 30716084 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTCTCACTACTATGCTTGCACGTCACCTAGACAAAAACACTATGGGTTA[T/A]TTACAGTGGYGCTGGGGAACTCAGTCTTCCATGAACACCAGCATCGTGAG
Long Flanking Sequence:
GTGAGTTCAGCACATCTCAGTGGTCTTTTAGTTGTTTAATTATTAATCCTTTAAGTATACACTGTTTTGGGGAAATTTAGTTGCAAGTTGATTGTATTGTATACTGAGACATTAGACGTGTCTGTAATTCATAATATGGTATATTGTGCGGAAATGCTATAAGAGAAGAGTATATTTCAACGTAATACTAGTCCTGGTAAGTATTGTCAATTTGTGAATACATATTTATCATTTTAAATGACAGGTGTGTATTTGAAAATAATTCAACTTGAGAGGACAACACTGACTTGTCTTTTTGCAATTTATTTATATACCATGAACAACAGAAAATCTATAATTGTTGTGCCATGAAAATATAATACCTTCACATGCCTCTGAGATGTATGTGTGTTTTTCAGCTTCACAACAGCTCATTGTGGCTTGCAGTTTTCATCGCGTGGCATACGGCCGGGTCTCACTACTATGCTTGCACGTCACCTAGACAAAAACACTATGGGTTA[T/A]TTACAGTGGCGCTGGGGAACTCAGTCTTCCATGAACACCAGCATCGTGAGGGACACCAAAAGCAGCCATTTCACATTTGCTGTGCAGGTAAGTTGCTGTTTTGATGTGACCATTTTGATTTTTTTGCCAACCACTTTTTTTGACGTACCACCTTTTGTATCATTCTAGTTGGGAATTCCACATACATTTATCATGATGAGCTACCAGTACAAATTCCAGGATGATGATCAGACCAAGATCAAGGGCTCTGTCAAGTATGTGTCTGTGGATTTCTGCCTTTTTGTAATATTTATTCTGTGATTCATATTCATTGACACAACTTTACATTTTGTATTATGACACTAGTGTCCAGTTAAATTATGTTTTCTAAGCAAAAATAATTATCATCAATTATAACCATGGTTTACAGTAGACGCTATAAAATGTTATTCATTGTTACAAGATTATGTACCAAAAAAATCCTGTTAGGCTTCTTTGGACAAAAATTATTTGATGACTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9129
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016096 | Nonsense | 314 | 563 | 9 | 16 |
Genomic Location (Zv9):
Chromosome 23 (position 30954867)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 30789757 |
GRCz11 | 23 | 30716288 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTGTATCATTCTAGTTGGGAATTCCACATACATTTATCATGATGAGCTA[C/A]CAGTACAAATTCCAGGATGATGATCAGACCAAGATCAAGGGCTCTGTCAA
Long Flanking Sequence:
TGTCAATTTGTGAATACATATTTATCATTTTAAATGACAGGTGTGTATTTGAAAATAATTCAACTTGAGAGGACAACACTGACTTGTCTTTTTGCAATTTATTTATATACCATGAACAACAGAAAATCTATAATTGTTGTGCCATGAAAATATAATACCTTCACATGCCTCTGAGATGTATGTGTGTTTTTCAGCTTCACAACAGCTCATTGTGGCTTGCAGTTTTCATCGCGTGGCATACGGCCGGGTCTCACTACTATGCTTGCACGTCACCTAGACAAAAACACTATGGGTTATTTACAGTGGCGCTGGGGAACTCAGTCTTCCATGAACACCAGCATCGTGAGGGACACCAAAAGCAGCCATTTCACATTTGCTGTGCAGGTAAGTTGCTGTTTTGATGTGACCATTTTGATTTTTTTGCCAACCACTTTTTTTGACGTACCACCTTTTGTATCATTCTAGTTGGGAATTCCACATACATTTATCATGATGAGCTA[C/A]CAGTACAAATTCCAGGATGATGATCAGACCAAGATCAAGGGCTCTGTCAAGTATGTGTCTGTGGATTTCTGCCTTTTTGTAATATTTATTCTGTGATTCATATTCATTGACACAACTTTACATTTTGTATTATGACACTAGTGTCCAGTTAAATTATGTTTTCTAAGCAAAAATAATTATCATCAATTATAACCATGGTTTACAGTAGACGCTATAAAATGTTATTCATTGTTACAAGATTATGTACCAAAAAAATCCTGTTAGGCTTCTTTGGACAAAAATTATTTGATGACTTTGAAAGAAGAATAATAGTGCATTTACAAAATACTAATTGTAATTTTAATATAATTGTATAATTTGCCACTATCCTAGGATTTGTTTGTTATGCTGTAAGAAGTTTGAAATATTTTAAAACATGCAGTTATTCTGATTTTACTTATTATATTATACACTTATTATATTTATAGGTGCAGTAGGTGATCTGATATCTTTGAAAACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24367
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016096 | Essential Splice Site | 465 | 563 | 13 | 16 |
Genomic Location (Zv9):
Chromosome 23 (position 30959665)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 30794555 |
GRCz11 | 23 | 30721086 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCAGGAGTCTGTGCGCAGAATTATCGAAGCAGAGGAGTCTAAGATGGG[T/A]ATGACAGCATAACTCCCAATAATGATCAAAGGGTGCATTTTTATTTGTTT
Long Flanking Sequence:
TGGGCCAATTGACTTCCTAGTACTCGTCTCCAACCTTTATCCCCCGCGAGTCTGGAAAATAATAGAGCGAAATCCTTTTAAATGGCTTTGAAAGTGTGAGTAAAAGAGCAAATGGTAAATTAACATCGAACCTTTGGTCTTTTGTTTAGGGAGCTGGAGAAGCAGCGGGAGAGTTCGGCGTCAGACGTTGCCAAGAAGAAGCAAGAGGCAGAAGCAGCTGTGAGTTCATAATGTCTAAATCCGCCGCAAATAATTTATAATGTGTGGCCGTTTAAAGTGGTCATAACTTTCACGGCAGGCGCTTTGTGTTGGGAGAAACAATGAGTTAGCGTCAGGCCATCGTTCCTATCTGCACATCAGTCGCTGTGTCAGGGTGATAAATGTGCGCCTTCACTATGTGCATATACAAGCAGTCTTATTTGAAATCACTCTTTTCTCTAGGTTCTGCTGATGCAGGAGTCTGTGCGCAGAATTATCGAAGCAGAGGAGTCTAAGATGGG[T/A]ATGACAGCATAACTCCCAATAATGATCAAAGGGTGCATTTTTATTTGTTTTTTTTGCCAAGTGGGGATTGGTTAGTAAGACGTCTTTCTTTTCTTTTTTCAGGTCTGATCATCCTCAATGCCTGGTATGGCAAGTTTGTGACGGACAACAGCCGTAAGCATGAAAGGGCAAGGGTCATTGATGTGACAGTGCCTCTACAGTGTCTGGTGAAGGACTCTAAGCTCATGCTCACAGAAGCATCTAAGGTAAAGCTCAGTTATGCCTGCTCTGTAATATTAGTCCAAAAGACAAATATTTTAATCTTTTTCAAAACTGTAAATTCACGTACAATTGAACACAAAATGCATATGCTTTAAAAGTTCTTTTATTTGTATAAAATTAGTACTTTCAACAAAGACCTTTAGTATTTTAAAAATGGTAATATAATTACTGCTTGGGTAAATGGTGTGAAAAGTTTAGCTTTTCCAACTTTTAAATTAGCCGTCACTGGAATATTACAG
Associated Phenotype:
Not determined